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Absence of PRKAG2 mutation in isolated familial Wolff-Parkinson-White syndrome - A case report
Chia Sung Wang
, Chia Ti Tsai
, Yen Hong Lin
, Kuan Lih Hsu
, Chuen Den Tseng
,
Jiunn Lee Lin
, Yi Lwun Ho
研究成果
:
雜誌貢獻
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文章
›
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1
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引文 斯高帕斯(Scopus)
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深入研究「Absence of PRKAG2 mutation in isolated familial Wolff-Parkinson-White syndrome - A case report」主題。共同形成了獨特的指紋。
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Medicine and Dentistry
Absence
100%
Autosomal Dominant Inheritance
16%
Chromosome 7
16%
Denaturing High Performance Liquid Chromatography
16%
Disease
50%
DNA Sequence
16%
Genetic Linkage
16%
Hydroxymethylglutaryl Coenzyme A Reductase Kinase
16%
Hypertrophic Cardiomyopathy
33%
Intron
16%
Polymerase Chain Reaction
16%
Single Nucleotide Polymorphism
16%
Ventricular Hypertrophy
16%
Wolff-Parkinson-White Syndrome
100%
Pharmacology, Toxicology and Pharmaceutical Science
Absence
100%
Disease
50%
Heart Ventricle Hypertrophy
16%
High Performance Liquid Chromatography
16%
Hydroxymethylglutaryl Coenzyme A Reductase Kinase
16%
Hypertrophic Cardiomyopathy
33%
Wolff Parkinson White Syndrome
100%
Biochemistry, Genetics and Molecular Biology
AMP-activated Protein Kinase
12%
Autosomal Dominant Inheritance
12%
Chromosome 7
12%
Denaturing High Performance Liquid Chromatography
12%
DNA Sequence
12%
Genetic Linkage
12%
Intron
12%
Polymerase Chain Reaction
12%
PRKAG2
100%
Single-Nucleotide Polymorphism
12%
Wolff-Parkinson-White Syndrome
100%
Neuroscience
AMP-activated Protein Kinase
12%
Chromosome 7
12%
DNA Sequencing
12%
Epileptic Absence
100%
Hypertrophic Cardiomyopathy
25%
Intron
12%
Polymerase Chain Reaction
12%
PRKAG2
100%
Single-Nucleotide Polymorphism
12%